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Validation of a liquid chromatographic method for the pharmaceutical quality control of products containing elacridar

Emilia Sawicki1, Michel J Hillebrand1, Hilde Rosing1

  • 1Department of Pharmacy & Pharmacology, The Netherlands Cancer Institute / Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Journal of Pharmaceutical Analysis
|February 7, 2018
PubMed

Keywords:
DissolutionGF120918HPLC–UVHydroxylationSolid dispersion

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